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Acta Pharmacologica Sinica (2009) 30: 1505–1512; doi: 10.1038/aps.2009.150
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| Original Article | [ Full text ] |
| Long-term baicalin administration ameliorates metabolic disorders and hepatic steatosis in rats given a high-fat diet |
Hong-xia GUO#,
Dai-hua LIU#, Ying MA, Jin-feng LIU, Ying WANG, Zhi-yan DU, Xin WANG, Jing-kang SHEN, Hong-li PENG*
State Key Laboratory of Drug Research, Shanghai
Institute of Materia Medica,
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Methods: Body weight was examined in high-fat diet (HFD)-fed rats with or without baicalin treatment. At the end of the experiment, serum biochemical parameters, liver histology and lipid profile were analyzed to assess whether the animals were suffering from metabolic disorders or hepatic steatosis. In the liver, the phosphorylation of AMP activated protein kinase (AMPK) and acetyl-CoA carboxylase (ACC) and the gene expression of some enzymes involved in lipogenesis were examined. The effects of baicalin on the phosphorylation of AMPK and lipid accumulation induced by high glucose in human hepatoma HepG2 cells were also examined.
Results: Baicalin (80 mg/kg) administered ip for 16 weeks
suppressed body weight gain in HFD-fed rats. Weight reduction was accompanied by the
reduction of visceral fat mass. Baicalin significantly decreased the elevated serum
cholesterol, free fatty acid and insulin concentrations caused by the HFD. Baicalin also
suppressed systemic inflammation by reducing the serum level of tumor necrosis
factor α. Baicalin reduced hepatic lipid accumulation, enhanced the phosphorylation of AMPK and ACC and down-regulated genes involved in lipogenesis,
including fatty acid synthase and its upstream
regulator SREBP
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Keywords:
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We thank Dr C AALKJAER for critically reading the
manuscript. This study was
supported by grants from the National Natural Science Foundation of China (No 30672467) and the Ministry of Science and
Technology (No 2007AA02Z308).
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